VISCUM QUERCUS 1% SPRAY [URIEL PHARMACY INC.]

VISCUM QUERCUS 1% SPRAY [URIEL PHARMACY INC.]
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NDC 48951-9322-2
Set ID 6c2a8386-cb0a-745e-e053-2a91aa0af0af
Category HUMAN OTC DRUG LABEL
Packager Uriel Pharmacy Inc.
Generic Name
Product Class
Product Number
Application Number
  • INDICATIONS & USAGE

    Directions: ONLY FOR USE AS A NASAL SPRAY.

  • DOSAGE & ADMINISTRATION

    Ages 12 and older: 2-3 sprays. Ages 2-11: 1-2 sprays. Under age 2: Consult a doctor.

  • ACTIVE INGREDIENT

    Active Ingredient: Viscum album
    (Quercus) 1X

  • INACTIVE INGREDIENT

    Inactive Ingredients: Distilled water, Sea
    salt, Grapefruit seed extract

  • PURPOSE

    Use: Temporary relief of headache.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN.

  • WARNINGS

    Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seals on box are broken or missing.

    SHAKE WELL BEFORE USE.
    REFRIGERATE AFTER OPENING.
    USE WITHIN 30 DAYS OF OPENING.

  • QUESTIONS

    Questions? Call 866.642.2858
    Uriel, East Troy, WI 53120
    www.urielpharmacy.com

  • PRINCIPAL DISPLAY PANEL

    ViscumQuercus1NasalSpray

  • INGREDIENTS AND APPEARANCE
    VISCUM QUERCUS 1% 
    viscum quercus 1% spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:48951-9322
    Route of AdministrationNASAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    VISCUM ALBUM FRUITING TOP (UNII: BK9092J5MP) (VISCUM ALBUM FRUITING TOP - UNII:BK9092J5MP) VISCUM ALBUM FRUITING TOP1 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    CITRUS PARADISI SEED (UNII: 12F08874Y7)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:48951-9322-230 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/01/2009
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic09/01/2009
    Labeler - Uriel Pharmacy Inc. (043471163)
    Establishment
    NameAddressID/FEIBusiness Operations
    Uriel Pharmacy Inc.043471163manufacture(48951-9322)

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